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Biotech & Drug DiscoveryKOSDAQ 1961702 approvals4 trials

Alteogen Inc.

Official website

KOSDAQ-listed biotech behind the Hybrozyme IV-to-SC platform and the Eyluxvi Eylea biosimilar.

As of 2026-10-10, Alteogen Inc. has 2 Korean MFDS drug approvals, 9 PubMed-indexed papers on record (counted by the MAA Company Index from its own matching of public databases).

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Business overview

Source: DART corporate disclosure

Founded in 2008 and listed on KOSDAQ in 2014, Alteogen is a biotech company specializing in biobetters and biosimilars. It out-licenses platform technologies to global pharmaceutical companies including MSD, AstraZeneca, GSK, Daiichi Sankyo, and Sandoz, including Hybrozyme™ (hyaluronidase technology converting IV to SC formulations), NexP™ (long-acting biologics fusion technology), and NexMab™ (antibody-drug conjugate technology). Its core asset ALT-B4 (berahyaluronidase alfa) was commercialized as a standalone injection (Tergase Inj.) in 2024; its Herceptin biosimilar was out-licensed to Qilu Pharmaceutical of China and commercialized there in 2024, generating royalty income; and its Eylea biosimilar Eyluxvi® completed global Phase 3 trials in 2024 and received European marketing authorization in September 2025.

Products & technology

  • ALT-B4 (berahyaluronidase alfa)Hyaluronidase enabling IV-to-SC formulation conversion
  • Tergase Inj. (ALT-B4 standalone injection)Standalone hyaluronidase injection for pain and swelling relief
  • Herceptin biosimilarAntibody biosimilar for breast cancer treatment
  • Eyluxvi (Eylea biosimilar)Antibody biosimilar for ophthalmic disease treatment

Regulatory approvals

data.go.kr

2 Korean MFDS drug approvals · 2024–2026

  • MFDS drugEYZANFY Injection(Aflibercept)2026-05-14
    Drug · Prescription · Approval202601428
  • MFDS drugTergase Injection(Berahyaluronidase alfa(Recombinant hyaluronidase))2024-07-05
    Drug · Prescription · Approval202401660

Clinical trials

data.go.kr

4 MFDS clinical trial authorisations · 2017–2021 (Phase 1 3 · Phase 1/2a 1)

  • Phase 1ALT-BB42021-09-15

    4 trial sites

  • Phase 1ALT-L92019-05-21

    4 trial sites

  • Phase 1/2aALT-P12017-07-11

    3 trial sites

  • Phase 1ALT-P72017-06-16

    2 trial sites

Global clinical trials

ClinicalTrials.gov · sponsor-matched

R&D and key agreements

Source: DART corporate disclosure

NexP™ 융합기술 · 플랫폼 기술 · Long-acting biologics fusion technology

NexMab™ (ADC 기술) · 플랫폼 기술 · Next-generation antibody-drug conjugate technology

Key disclosures

KRX KIND via OpenDART
Show 10 more events

Publications

PubMed · affiliation-matched

Patents

KIPRIS · applicant-matched
Show 150 more patents

AI reads

MAA server logs · IP-verified
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Measured since Aug 27, 2026 · 5 AI engines · last read Oct 8, 2026

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Sources and updates

Counts on this page are not company-reported figures. MAA matched records from DART, the Korean MFDS, the US FDA, ClinicalTrials.gov, PubMed and KIPRIS to this company itself, by business registration number or registered name, never by name similarity. They may differ from figures the company publishes.

Company basics
Korea Exchange · DART
Business content
Compiled from disclosure filings
Approvals & clinical trials
Korean MFDS (data.go.kr) · US FDA openFDA — updated weekly
Key disclosures
KRX KIND via OpenDART exchange filings — updated daily
Global clinical trials
ClinicalTrials.gov (US NIH) — sponsor-matched, updated weekly
Financials
DART corporate disclosure filings — annual
Publications
PubMed (US National Library of Medicine) — affiliation-matched, updated daily
Patents
KIPRIS (Korea Institute of Patent Information) — applicant-matched, updated monthly
AI reads
Our server logs, IP-verified every 6 hours
AI visibility
Measured 2026-10-01

This page is compiled from public sources without the company's involvement. If anything is inaccurate or incomplete, please let us know. Materials provided by the company are labelled as such.

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